SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2696 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216884 | GAGGTGGGAGGAGGG[C/G]AGAAGTGAAGGAAGA | 50717 |
rs750936 | snp | A/G | 0.489608 | 0.0713316 | intron-variant | DCAF8 | GRCh38.p7 | 1:160237740 | AGATGGGGTCTTGCT[A/G]TATTGCCCAGGCTGG | 50717 |
rs756311 | snp | A/T | 0.439918 | 0.162576 | intron-variant | DCAF8 | GRCh38.p7 | 1:160235050 | GTAAAATATAAATTA[A/T]TTTATATTGGGGAAT | 50717 |
rs947492 | snp | A/G | 0.497359 | 0.0362457 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246738 | TGCCTCGGCCTCCCA[A/G]TGTGCTGGGATTATA | 50717 |
rs947493 | snp | C/T | 0.442113 | 0.159977 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246404 | TTTAATTCTACTTAC[C/T]TTTATCATCTGTGCA | 50717 |
rs947494 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263016 | TTTACCCACACCACC[C/T]CTCTTCAGAAAAGAG | 50717 |
rs947495 | snp | C/T | 0.441841 | 0.160303 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262886 | CTTAAGGAAACAAAG[C/T]CCTGAAAGGAAACGG | 50717 |
rs947496 | snp | A/T | 0.441568 | 0.160629 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160262716 | AACTCGCATTTGTTT[A/T]GAGTATCACAAGATA | 50717 |
rs1053553 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216900 | GAGGGAGGCTGGGAA[A/G]AGGTGGGAGGAGGGG | 50717 |
rs1053572 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160215998 | CACAAGATCCAACCA[A/G]GAATTCTGTATCCTG | 50717 |
rs1061511 | snp | G/T | 0.43978 | 0.162738 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219710 | AAGGCCTGCCTGCTG[G/T]AGTTTATTTCTTTTG | 50717 |
rs1132881 | snp | A/G | 0.126564 | 0.217402 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216505 | TTTGGTGTAGGGGTT[A/G]GGAAAAACAGGAAAT | 50717 |
rs1134572 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | DCAF8 | GRCh38.p7 | 1:160217929 | ATTGGCTTGCAGCCA[C/T]ACCCATTCTGTGTAT | 50717 |
rs1139189 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160253419 | ttgggaggccaaggc[A/G]ggtggatcgcctgag | 50717 |
rs1539245 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160228127 | agacacagtcttgct[A/T]tattgcccaagttgg | 50717 |
rs1573013 | snp | C/G | 0.442249 | 0.159814 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231716 | TTACTGTGTTGGACT[C/G]CAGCTAAACTGAGGC | 50717 |
rs1815703 | snp | A/G | 0.488485 | 0.0749998 | intron-variant | DCAF8 | GRCh38.p7 | 1:160245904 | TGATCTGCCCTCCTC[A/G]GCCTCCCAAAGTGCT | 50717 |
rs2096144 | snp | C/G | 0.441977 | 0.16014 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246905 | GTGGTATAATCACAG[C/G]TCACTGCAGCCTCAA | 50717 |
rs2275700 | snp | A/G | 0.441705 | 0.160466 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244237 | CCTCCCCAAAAATAT[A/G]TCATTATATGGATTT | 50717 |
rs2275701 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, downstream-variant-500B | DCAF8 | GRCh38.p7 | 1:160238850 | GTTTCCAGCTGTCAT[A/G]TAAGAAAAGGGGGTA | 50717 |
rs2275702 | snp | A/G | 0.017689 | 0.0923665 | synonymous-codon, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160238649 | CACACAGTGTTGCAA[A/G]AATACAAAACGTGTG | 50717 |
rs2369473 | snp | A/C | 0.488606 | 0.0746142 | intron-variant | DCAF8 | GRCh38.p7 | 1:160240937 | TGGGAGGCCGAGGCA[A/C]GTGGATCACGAGGTT | 50717 |
rs3189630 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | PEA15, DCAF8 | GRCh38.p7 | 1:160215309 | CCCCTATCTTGTGCT[C/T]TTCTGTCTGCAGTGT | 50717 |
rs3747624 | snp | A/G | 0.0177 | 0.0923944 | intron-variant | DCAF8 | GRCh38.p7 | 1:160231455 | ACTCCAAAAGATCCA[A/G]ATGGTCATGGCAAAG | 50717 |
rs3898317 | snp | A/G | 0.489024 | 0.0732638 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160264364 | GGGTTGGGAGCATAG[A/G]AGGAGGGGAGAGACA | 50717 |
rs4535996 | snp | A/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216348 | tCTTCTGTCACAAAG[A/T]ACCACAATAGTCTGC | 50717 |
rs4596880 | snp | A/T | 0.488485 | 0.0749998 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254910 | CCACCTGCTTTTGAG[A/T]TTTTCTTTTGTAAAA | 50717 |
rs4656252 | snp | A/G | 0.120326 | 0.21374 | downstream-variant-500B | PEA15, DCAF8 | GRCh38.p7 | 1:160215472 | CCCAGAATAAGGGCT[A/G]GGAAAATACCCCAAG | 50717 |
rs4656892 | snp | A/G | 0.444133 | 0.157519 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250423 | gtgagccaagatcgc[A/G]ccattgcactccagc | 50717 |
rs4656893 | snp | A/C | 0.0341735 | 0.126361 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250652 | TCTCACTTGAAAACG[A/C]AAGTGCTGAAAGGAT | 50717 |
rs6663516 | snp | G/T | 0.126909 | 0.217598 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263510 | ccggcatggtggagc[G/T]cgcctgcaatcccag | 50717 |
rs6670084 | snp | C/T | 0.488424 | 0.0751925 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247703 | catcaagttggcatt[C/T]gaaaagtttcagatt | 50717 |
rs6675318 | snp | A/C | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224046 | CCTCTTCTGCCTCAT[A/C]TAAAAGAATTGTTTA | 50717 |
rs6683068 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244310 | TGATTTTTCAGATGC[A/G]AAAGTGGGAACTAAA | 50717 |
rs6683177 | snp | A/G | 0.14665 | 0.227637 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244423 | AGCATTGCCCCCTAG[A/G]CAAGAATCTTCCAAT | 50717 |
rs6686429 | snp | C/T | 0.126564 | 0.217402 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258430 | CCACTCTAATCATCC[C/T]AGGAAATACTACCTA | 50717 |
rs6687974 | snp | A/G | 0.441568 | 0.160629 | intron-variant | DCAF8 | GRCh38.p7 | 1:160254183 | AAAAATAAGCTAGGT[A/G]TGGTGGTGCATGCCT | 50717 |
rs6688586 | snp | A/C | 0.489259 | 0.0724914 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263555 | gaggcaggagaattg[A/C]ttgaacccggaggcg | 50717 |
rs6690637 | snp | A/C | 0.441568 | 0.160629 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260466 | CCAGTGTCACTCAAT[A/C]TTTTCCTACTACAAA | 50717 |
rs6701228 | snp | C/G | 0.0629771 | 0.165899 | intron-variant | DCAF8 | GRCh38.p7 | 1:160260071 | AACTTATTCAAAGCT[C/G]TATCAATGATGTGCA | 50717 |
rs6703880 | snp | A/C | 0.440057 | 0.162414 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263930 | gtccatcTACTAGAT[A/C]TTTACTAGACTTGAG | 50717 |
rs7517599 | snp | A/C | 0.499824 | 0.00938333 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236263 | GAGGCATCACACACA[A/C]ACACACACACACATA | 50717 |
rs7538782 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF8 | GRCh38.p7 | 1:160232595 | ccagtggaccaagat[C/G]gtgccactgcactcc | 50717 |
rs9633341 | snp | A/G | 0.489665 | 0.0711382 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236604 | ACCTAGGTCTGCCTG[A/G]ATCCAAACAAGATGT | 50717 |
rs9660289 | snp | C/G | 0.45866 | 0.137698 | intron-variant | DCAF8 | GRCh38.p7 | 1:160255806 | TATATTTTTAGTAGA[C/G]ACAGGGTTTTGCTAT | 50717 |
rs9661510 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260098 | TGCAAAAAAAAAAAa[A/C]caaaaaacaacattt | 50717 |
rs9662568 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160260100 | CAAAAAAAAAAAACC[A/C]AAaaacaacattttt | 50717 |
rs10494338 | snp | C/T | 0.031825 | 0.122064 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257181 | GTCACTACCCCATGC[C/T]TATTGCTGATTCAAT | 50717 |
rs10494339 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF8 | GRCh38.p7 | 1:160257478 | TAGTCACTTTATGAT[C/T]TTAAAAGCCTATTAC | 50717 |
rs10660397 | in-del | -/A/AA/AAA | 0.487621 | 0.0776941 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234242 | GTGAGACTGCACCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 50717 |
rs10732269 | snp | A/T | 0.439918 | 0.162576 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226932 | TCATATATCCGTGTG[A/T]AAGGTGGTAGTTAAA | 50717 |
rs10908770 | snp | C/G | 0.439363 | 0.163222 | intron-variant | DCAF8 | GRCh38.p7 | 1:160219982 | GGACCAACCACCTCC[C/G]CTGCCTCACCTGCAC | 50717 |
rs10908771 | snp | C/G | 0.441977 | 0.16014 | intron-variant | DCAF8 | GRCh38.p7 | 1:160246931 | ACCACTTCTCTCCAG[C/G]CAGGACGACAGAGCA | 50717 |
rs10908772 | snp | C/T | 0.441432 | 0.160792 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253288 | GGAGGATCGCTTGAG[C/T]CCAGGAATTTGAGAC | 50717 |
rs11265356 | snp | C/T | 0.148326 | 0.228391 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217103 | GACAGTTGGCTCCCC[C/T]CCCACCCCCAGCAAC | 50717 |
rs11265357 | snp | A/G | 0.0711525 | 0.174681 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217383 | TATGCACCTCTCCAT[A/G]GAGCCCCATTCCAGG | 50717 |
rs11265358 | snp | C/T | 0.147991 | 0.228242 | intron-variant | DCAF8 | GRCh38.p7 | 1:160218128 | ACACATGGACGGCAA[C/T]GGACAAAAGTAGATA | 50717 |
rs11265359 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221639 | GTTCCCCACAGCTAA[A/G]AAGGAATAAAAAGGA | 50717 |
rs11265360 | snp | G/T | 0.148326 | 0.228391 | intron-variant | DCAF8 | GRCh38.p7 | 1:160228746 | AGCTATTTCTCTATA[G/T]TCCCTTGAAGTAATT | 50717 |
rs11265361 | snp | C/T | 0.441841 | 0.160303 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242182 | CCTGGGAGGTGGAGG[C/T]TGCAGTGAGCCGAGA | 50717 |
rs11265362 | snp | C/T | 0.134802 | 0.221877 | intron-variant | DCAF8 | GRCh38.p7 | 1:160242910 | CTCTAGAACCCTGTG[C/T]CTTTCAACTAAACCC | 50717 |
rs11265363 | snp | A/C | 0.459233 | 0.136827 | intron-variant | DCAF8 | GRCh38.p7 | 1:160244618 | CCTATTATTATTATT[A/C]TTTCTTTTTTTTTTT | 50717 |
rs11265364 | snp | C/T | 0.488424 | 0.0751925 | intron-variant | DCAF8 | GRCh38.p7 | 1:160247179 | AGCTGATGAGCTCAC[C/T]GTCCCAGGTAGTTGG | 50717 |
rs11265365 | snp | C/T | 0.161596 | 0.233848 | intron-variant | DCAF8 | GRCh38.p7 | 1:160259305 | tttgggaggctgagg[C/T]gggcagatcacaagg | 50717 |
rs11284812 | in-del | -/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160256013 | CAGAACTAAGCAAAC[-/T]TTTTTTTTTTTTTTT | 50717 |
rs11375715 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | DCAF8 | GRCh38.p7 | 1:160258758 | CAAAAATAAAAAAAA[-/A]CTTTAGAAAGATAAA | 50717 |
rs11455653 | in-del | -/A | 0.5 | 0 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263490 | AAAAAAAAAAAAAAA[-/A]TTACCCGGCATGGTG | 50717 |
rs11591179 | snp | C/T | 0.444799 | 0.156695 | intron-variant | DCAF8 | GRCh38.p7 | 1:160236277 | AAACACACACACACA[C/T]ACATACACGTACGTA | 50717 |
rs12071837 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160248709 | tccatctcaaaaaaa[A/G]aaaaaaaaaaaaCTG | 50717 |
rs12075010 | snp | A/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160258758 | CTATCTCTACAAAAA[A/T]AAAAAAAACTTTAGA | 50717 |
rs12082427 | snp | C/T | 0.161596 | 0.233848 | intron-variant | DCAF8 | GRCh38.p7 | 1:160249007 | ggctggcctgaccaa[C/T]gtggtaaaaccccat | 50717 |
rs12091372 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226552 | TCCAATCTCAGAGCC[A/G]ATCTCTTGAAAAATG | 50717 |
rs12096571 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234931 | CCAAGCCTAAAACAT[G/T]TCTATCTTTTAAGCA | 50717 |
rs12128926 | snp | G/T | 0.0115144 | 0.0749975 | upstream-variant-2KB | DCAF8 | GRCh38.p7 | 1:160263634 | tggaatgagactccg[G/T]ctcaaaaaaaaagta | 50717 |
rs12130998 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF8 | GRCh38.p7 | 1:160250406 | ggaaggcggaggttg[C/T]ggtgagccaagatcg | 50717 |
rs12145552 | snp | G/T | 0.00716713 | 0.0594884 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227392 | gcctcaacctgccgc[G/T]tagctgggactacag | 50717 |
rs12403037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226004 | acacaccaccacgcc[C/T]ggccaatttttgtat | 50717 |
rs12566097 | snp | C/T | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160253377 | cacagtggctgacgt[C/T]taagtgacgctggta | 50717 |
rs12728099 | snp | A/G | 0.0141169 | 0.0828202 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230532 | TCACTATGGATAAAA[A/G]AAAGTGGTAGCTCAG | 50717 |
rs12730809 | snp | A/C | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160256366 | GTACAACTTACAATA[A/C]AACATTAAAGAGAGG | 50717 |
rs12742133 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221186 | AAATGCTGGCCTGGG[A/G]GAGGGCATTCAGCCC | 50717 |
rs12746884 | snp | A/G | 0.5 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221840 | aaaaaaaaaaaaaaa[A/G]GATAAGGTTAACCAG | 50717 |
rs12759667 | snp | A/G | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221187 | AATGCTGGCCTGGGA[A/G]AGGGCATTCAGCCCT | 50717 |
rs12760305 | snp | A/C | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160242205 | agccgagattgtgcc[A/C]ccgtactccagcttg | 50717 |
rs12760784 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221209 | TTCAGCCCTGCATCT[C/T]TCTGGAACAGAATGC | 50717 |
rs12760786 | snp | C/T | | | intron-variant | DCAF8 | GRCh38.p7 | 1:160221211 | CAGCCCTGCATCTCT[C/T]TGGAACAGAATGCAA | 50717 |
rs12760935 | snp | C/T | 0 | 0 | intron-variant | DCAF8 | GRCh38.p7 | 1:160221278 | CTTCTGACTTCCTTT[C/T]TCTAAATGCCTATTG | 50717 |
rs16831606 | snp | A/G | 0.0433465 | 0.140692 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216083 | GGACTTTCAGACTCA[A/G]TGACCAGTGATAAGA | 50717 |
rs16831610 | snp | A/T | 0.0433465 | 0.140692 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216260 | AGTTGGATGGCTTAA[A/T]GATCAAGCAGCTAAA | 50717 |
rs16831617 | snp | C/T | 0.0441095 | 0.141807 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160216983 | TAATCAAGTGCAAAA[C/T]ACTGTGGTAAGTACA | 50717 |
rs16831619 | snp | A/G | 0.0441095 | 0.141807 | utr-variant-3-prime, nc-transcript-variant | DCAF8 | GRCh38.p7 | 1:160217011 | ACAGAGAATGAATAA[A/G]GTGGAAAGGAAAGTG | 50717 |
rs16831628 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | DCAF8 | GRCh38.p7 | 1:160223267 | AGGGCTCCACTCTCC[A/G]GAATCAGTAAAAGAA | 50717 |
rs16831632 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224136 | TAAAGAGGGCTTTCC[C/T]TGACTCCCTAACAAG | 50717 |
rs16831634 | snp | C/T | 0.0210248 | 0.100351 | intron-variant | DCAF8 | GRCh38.p7 | 1:160224560 | GAGCTCTGCCAAGAA[C/T]AAGAACATAGCAGTG | 50717 |
rs16831635 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226232 | CCTACCGAAAAAGGT[C/T]ACTCACGGGCAGAAA | 50717 |
rs16831636 | snp | A/C | 0.0655868 | 0.168795 | intron-variant | DCAF8 | GRCh38.p7 | 1:160226634 | AACCTCTTCCTCATC[A/C]CCAGCTGGCCACTTT | 50717 |
rs16831647 | snp | C/T | 0.247053 | 0.249983 | intron-variant | DCAF8 | GRCh38.p7 | 1:160227162 | GAGCTGAAGACTGAG[C/T]TACTGGAGAACATCA | 50717 |
rs16831650 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230497 | AGTGTTAACAAAAGG[C/T]GTTCACGGTAACAAA | 50717 |
rs16831651 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | DCAF8 | GRCh38.p7 | 1:160230633 | CCAGTATTTAAAATT[C/T]CTAGTGCACGTTTAT | 50717 |
rs16831658 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | DCAF8 | GRCh38.p7 | 1:160234557 | GCACCAGATTCAATT[C/G]CTGGTGGCCTAACAG | 50717 |